Lina Finkel

22q11.2 duplication syndrome: Two new familial cases with some overlapping features with DiGeorge/velocardiofacial syndromes

M. Portnoï, N. Gruchy, V. Malan, 2005, American journal of medical genetics. Part A.

Cryptic Xp duplication including the SHOX gene in a woman with 46,X, del(X)(q21.31) and premature ovarian failure.

N. Bourcigaux, G. Tachdjian, S. Christin‐Maitre, 2007, Human reproduction.

Midline defects in deletion 18p syndrome: clinical and molecular characterization of three patients

F. Denoyelle, Y. Le Bouc, J. Siffroi, 2007, Clinical dysmorphology.